Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_provenance.
- NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_provenance.
- NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_assertion evidence source_evidence_literature NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_provenance.
- NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_assertion SIO_000772 16895480 NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_provenance.
- NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_assertion wasDerivedFrom befree-2016 NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_provenance.
- NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_assertion wasGeneratedBy ECO_0000203 NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_provenance.
- befree-2016 importedOn "2016-02-19" NP563317.RAtyZuntzVcjro-qruhpB5B3gi-159RVCPTxhQgYasrlI130_provenance.